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87-90-1 - Trichloroisocyanuric acid, 90+% - Isocyanuric chloride - Symclosene - B23906 - Alfa Aesar

B23906 Trichloroisocyanuric acid, 90+%

Numéro CAS
Isocyanuric chloride

Dimensions Prix ($) Quantité Disponibilité
100g 18,90
500g 45,70
2500g 172,00
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Trichloroisocyanuric acid, 90+%


Propriétés chimiques

Poids formulaire
Point de fusion
ca 245° dec.
Point d'éclair
Moisture Sensitive
Soluble in chlorocarbon, acetonitrile, acetone, water (12 g/L).


Trichloroisocyanuric acid was used as a disinfection reagent in the transformation of benzophenone-3 in chlorinated water. It was also used in the synthesis of 2-halomethylene-3-oxoketoximes. It is used as a bleaching agent in the textile industry, a reagent in organic synthesis.


Moisture sensitive. Store away from reducing agents, acids, bases, flammable substances, organic materials, light, water/ moisture.

Références bibliographiques

Ulf Tilstam and Hilmar Weinmann. Trichloroisocyanuric Acid:? A Safe and Efficient Oxidant. Org. Proc. Res. Dev. 2002, 6 (4), 384-393.

Ardeshir Khazaei; Mohammad Ali Zolfigol; Amin Rostami; Arash Ghorbani Choghamarani. Trichloroisocyanuric acid (TCCA) as a mild and efficient catalyst for the trimethylsilylation of alcohols and phenols with hexamethyldisilazane (HMDS) under heterogonous conditions. Catalysis Communications. 2007, 8 (3), 543-547.

Low-cost chlorinating and oxidizing agent; review: Org. Process Res. Dev., 6, 384 (2002). Aromatic compounds can be chlorinated either on the ring (ionic conditions) or on the side chain (free-radical conditions): J. Org. Chem., 35, 719 (1970). In the presence of BF3 etherate, ketones are ɑ-chlorinated at the more substituted position: Synth. Commun., 15, 385 (1985). In combination with pyridine, sulfides are selectively oxidized to sulfoxides: Synth. Commun., 31, 245 (2001), thiols to disulfides: Synth. Commun, 31, 1825 (2001), and secondary alcohols to ketones: Synth. Commun., 22, 1589 (1992). In the presence of methanol in acetonitrile, acetone or dichloromethane, the same reagent system converts aldehydes directly to methyl esters: Synth. Commun., 26, 2633 (1996). Effective co-oxidant for the TEMPO-catalyzed chemoselective oxidation of alcohols to aldehydes and ketones: Org. Lett., 3, 3041 (2001). In acetic acid, pyridines are converted to their N-oxides: Synth. Commun., 34, 247 (2004).

With NaNO2 and wet silica selective mononitration of phenols is accomplished under mild conditions: Synlett, 191 (2003). Effectively catalyzes both the protection and deprotection of alcohols as their tetrahydropyranyl ethers: Synth. Commun., 34, 3623 (2004).

For a brief feature on uses in synthesis, see: Synlett, 2265 (2005).

Note: Confusion with Cyanuric chloride, L03442, exists in some earlier Fieser references.

Mentions de danger et de prudence du SGH

Mentions de danger (UE): H272-H302-H319-H335

May intensify fire; oxidizer. Harmful if swallowed. Causes serious eye irritation. May cause respiratory irritation.

Mentions de prudence: P221-P210v-P220-P261-P280a-P305+P351+P338-P304+P340-P301+P312a-P405-P501a

Take any precaution to avoid mixing with combustibles. Keep/Store away from clothing/combustible materials. Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves and eye/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. IF SWALLOWED: Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Autres références

Classe de danger
Groupe d'emballage
Code tarifaire harmonisé


Consulté récemment

Produits chimiques

Sciences de la vie

Métaux et matériaux


Analytique et matériel de laboratoire